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FDA 510(k) Applications Submitted by JENNIFER S PORTUGAL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012482
08/02/2001
STORZ MODULITH SLK LITHOTRIPTER WITH MULTIVIEW OPTION
KARL STORZ ENDOSCOPY-AMERICA, INC.
K011700
06/01/2001
MODULITH SLK LITHOTRIPTER
KARL STORZ ENDOSCOPY
K004037
12/28/2000
X-RAY SYSTEM XR-MX
KARL STORZ ENDOSCOPY
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